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DJO SURGICAL 498-28-048Recalls & reported problems

Encore Medical, L.P. · Ceramic Liner - Size 28 · Class 3 · Implant

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00888912087537), received between Nov 29, 2021 and Nov 29, 2021 — classified as 1 injury.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Device problems

  • Appropriate Device Problem Term/Code Not Available1

Patient problems

  • Insufficient Information1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryNov 29, 2021Appropriate Device Problem Term/Code Not Available

    REVISION SURGERY - DUE TO UNKNOWN REASON.

    Patient problems: Insufficient Information

    MAUDE report 12882836 ↗

Other Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic/Metal, Cemented Or Uncemented devices

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Sources and updates

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